FDA Inspection 959800 — Integra Microfrance

Integra Microfrance — FEI 3003249645

The FDA completed an inspection of Integra Microfrance on Feb 18, 2016 in St Aubin Le Monial. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 18, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
St Aubin Le Monial (France)